84857-13-6

Basic information

• Product Name: 2-amino-4-(4-fluorophenyl)-6-phenylpyrimidine
• Synonyms: 2-amino-4-(4-fluorophenyl)-6-phenylpyrimidine
• CAS NO: 84857-13-6
• Molecular Weight: 265.29
• Mol File: 84857-13-6.mol
• Article Data: 16

Chemical Properties

• CAS DataBase Reference: 2-amino-4-(4-fluorophenyl)-6-phenylpyrimidine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-amino-4-(4-fluorophenyl)-6-phenylpyrimidine(84857-13-6)
• EPA Substance Registry System: 2-amino-4-(4-fluorophenyl)-6-phenylpyrimidine(84857-13-6)

Safety Data

• Hazardous Substances Data: 84857-13-6(Hazardous Substances Data)

Upstream product

• 593-85-1 diguanidine carbonate 
• 459-57-4 4-fluorobenzaldehyde 
• 98-86-2 acetophenone 
• 459-56-3 4-fluorobenzylic alcohol 
• 113-00-8 guanidine nitrate 
• 536-74-3 phenylacetylene 
• 766-98-3 1-ethynyl-4-fluorobenzene 
• 100-51-6 benzyl alcohol 
• 50-01-1 guanidine hydrochloride 
• 403-41-8 1-(4-Fluorophenyl)ethanol 
• 98-85-1 1-Phenylethanol 
• 506-93-4 guanidine nitrate 
• 1608-51-1 4-fluorochalcone 
• 100-52-7 benzaldehyde 

Downstream Products

• 1202251-20-4 N-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-N'-(4'-(p-fluorophenyl)-6'-diphenylpyrimidin-2'-yl)thiourea 
• 1223546-47-1 C₁₈H₁₃ClFN₃O 
• 1236151-05-5 3-(4'-(4''-fluorophenyl)-6'-phenylpyrimidin-2'-yl)-2-phenylthiazolidin-4-one 
• 2387-23-7 1,3-Dicyclohexylurea 
• 1377325-03-5 C₂₃H₂₄FN₅O 
• 1446752-09-5 C₂₆H₁₉ClFN₃O₂ 
• 1446751-99-0 C₂₆H₂₀FN₃O₂ 
• 1446751-89-8 C₂₄H₁₈FN₃O 
• 1427026-58-1 C₃₆H₃₅FN₆O 

Relevant articles and documents

Iron-Catalyzed Alkyne-Based Multicomponent Synthesis of Pyrimidines under Air

An iron-catalyzed sustainable, economically affordable, and eco-friendly synthetic protocol for the construction of various trisubstituted pyrimidines is described. A wide range of trisubstituted pyrimidines were prepared using a well-defined, easy to prepare, bench-stable, and phosphine-free iron catalyst featuring a redox-noninnocent tridentate arylazo pincer under comparatively mild aerobic conditions via dehydrogenative functionalization of alcohols with alkynes and amidines.

Iron Catalyzed Synthesis of Pyrimidines Under Air

Herein we report an iron-catalyzed multicomponent dehydrogenative functionalization of alcohols to pyrimidines under atmospheric conditions. Using a well-defined Fe(II)-complex featuring redox noninnocent 2-phenylazo-(1,10-phenanthroline) ligand, as a cat

One-Pot Three-Component Synthesis of 2-Amino Pyrimidines in Aqueous PEG-400 at Ambient Temperature

Amino pyrimidines have been synthesized by a one-pot procedure under environmentally friendly reaction conditions at room temperature. The use of aqueous PEG-400 circumvents the problems associated with the toxic, hazardous organic solvents and oxidizing agents.